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1.5 million people annually are harmed from drug errors. Don't Risk Your Health! Ask a Health Expert Now

From simple mix-ups to fatal overdoses, medication mistakes happen, on average, once a day to every hospital patient, a new report says. Nationwide, at least 1.5 million people annually are harmed from drug errors, more than half of them in nursing homes.
Many Unfavorable Drug Studies Aren’t Published. Nearly a third of antidepressant drug studies are never published in the medical literature, and nearly all of those happen to show that the drug being tests failed to work.
Only Drugs That are Safe Should be put on the Market. Drug developers are just beginning to come to grips with recent FDA oversight reforms and how they will affect drug safety. But, it appears that industry and consumer advocates are not together on how well the overhaul will be able to prevent future drug safety scandals.

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Review Coniel Safety Reports submitted to FDA

Total Coniel reports: 3.
Coniel FDA safety alerts: No.
Reported deaths: 3    Reported hospitalizations: 3.
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FDA Reported Coniel Side Effects: blood urea increased, blood sodium decreased, blood potassium increased, blood culture positive, blood creatinine increased, blood cholesterol increased, blood albumin decreased, asthenia, ascites.
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Coniel Side Effects Report #5115518-6
Physician from JAPAN reported CONIEL problem on May 18, 2006. Female patient, 75 years of age, weighting 127.9 lb, was diagnosed with hypertension, asthma, gastritis, musculoskeletal pain, dysthymic disorder and was treated with CONIEL. After drug was administered, patient experienced the following problems/side effects: ascites, asthenia, blood albumin decreased, blood cholesterol increased, blood creatinine increased, blood culture positive, blood potassium increased, blood sodium decreased, blood urea increased. CONIEL dosage: 8 MG, UNK. During the same period patient was treated with PREDNISOLONE, FAMOTIDINE, HYPEN, TRYPTANOL, LEVOTOMIN, MEILAX, DIOVAN. Patient was hospitalized. Patient died on 07/03/2006.

Coniel Side Effects Report #5133418-2
CONIEL problem was reported by a Physician from JAPAN on May 18, 2006. Female patient, 75 years of age, weighting 127.9 lb, was diagnosed with hypertension, asthma, gastritis, musculoskeletal pain, dysthymic disorder and was treated with CONIEL. After drug was administered, patient experienced the following problems/side effects: ascites, asthenia, blood albumin decreased, blood cholesterol increased, blood creatinine increased, blood culture positive, blood potassium increased, blood sodium decreased, blood urea increased. CONIEL dosage: 8 MG, UNK. During the same period patient was treated with PREDNISOLONE, FAMOTIDINE, HYPEN, TRYPTANOL, LEVOTOMIN, MEILAX, DIOVAN. Patient was hospitalized. Patient died on 07/03/2006.

Coniel Side Effects Report #5153789-0
Physician from JAPAN reported CONIEL problem on May 18, 2006. Female patient, 75 years of age, weighting 127.9 lb, was diagnosed with hypertension, asthma, gastritis, musculoskeletal pain, dysthymic disorder and was treated with CONIEL. After drug was administered, patient experienced the following problems/side effects: ascites, asthenia, blood albumin decreased, blood cholesterol increased, blood creatinine increased, blood culture positive, blood potassium increased, blood sodium decreased, blood urea increased. CONIEL dosage: 8 MG, UNK. During the same period patient was treated with PREDNISOLONE, FAMOTIDINE, HYPEN, TRYPTANOL, LEVOTOMIN, MEILAX, DIOVAN. Patient was hospitalized. Patient died on 07/03/2006.

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